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1.
001-es BibID:
BIBFORM123875
Első szerző:
Espinosa-Ortega, Fabricio
Cím:
Autoantibodies and damage in patients with idiopathic inflammatory myopathies : a longitudinal multicenter study from the MYONET international network / Espinosa-Ortega Fabricio, Lodin Karin, Dastmalchi Maryam, Vencovsky Jiri, Diederichsen Louise P., Shinjo Samuel Katsuyuki, Danieli Maria Giovanna, Selva-O'Callaghan Albert, de Visser Marianne, Griger Zoltan, Ceribelli Angela, Gómez-Martin Diana, Andersson Helena, Mercado Mónica Vázquez-Del, Chinoy Hector, Lilleker James B., New Paul, Krogh Niels S., Lundberg Ingrid E., Alexanderson Helene, MYONET Registry Study Group
Dátum:
2024
ISSN:
0049-0172
Megjegyzések:
Objective To study the trajectories of changes in damage over time and explore associations with autoantibody defined subgroups using a large international cohort of patients with idiopathic inflammatory myopathies (IIM). Methods Data from the MYONET registry, including patients who were tested for autoantibodies and had at least one assessment of damage using the Myositis Damage Index (MDI), were analyzed. Patients were sub-grouped according to their autoantibody profiles (myositis-specific, myositis-associated, or seronegative). The index date was defined as the time point for the first registered MDI assessment. The longitudinal trajectories of damage with autoantibody status as the main predictor were analyzed using linear mixed models. Results A total of 757 adult patients were included in this study. Each year of disease duration since diagnosis had an estimated MDI score increase of 0.16 units for the seronegative group (reference). Compared with the seronegative group as reference, patients with dermatomyositis-specific autoantibodies developed less damage per year of follow-up since diagnosis (average 0.08 less score, P = 0.04), whereas patients with anti-PM/Scl autoantibodies developed more damage per year of follow-up since diagnosis (average 0.28 higher score, P = 0.03) independent of sex and age at diagnosis. The seronegative subgroup and the immune-mediated necrotizing myopathy autoantibody subgroup had the strongest correlation between severity of muscle damage and HAQ-DI scores at five years of follow-up, rho=0.84, P < 0.001 and rho=0.72, P < 0.001, respectively. Conclusion Our study is the first to describe patterns and trajectories of change in damage over time in relation to autoantibody defined subgroups in a large international multicenter cohort of patients with IIM. Patients with anti-PM/Scl scored a greater extent of damage, whereas patients with dermatomyositis-specific antibodies had less damage than seronegative patients. Severity in muscle damage had moderate to strong correlation with functional disability among the IMNM and seronegative subgroups with lower correlations for the other subgroups. These findings suggest that autoantibodies may be useful predictors of long-term damage.
Tárgyszavak:
Orvostudományok
Klinikai orvostudományok
idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
Autoantibodies
Dermatomyositis
Inflammatory myopathies
Organ damage
Myositis
Megjelenés:
Seminars In Arthritis And Rheumatism. - 68 (2024), p. 1-10.-
További szerzők:
Lodin, Karin
Dastmalchi, Maryam
Vencovsky, Jiri
Diederichsen, Louise Pyndt
Shinjo, Samuel Katsuyuki
Danieli, Maria Giovanna
Selva-O'Callaghan, Albert
de Visser, Marianne
Griger Zoltán (1979-) (belgyógyász, allergológus és klinikai immunológus, reumatológus)
Ceribelli, Angela
Gómez-Martin, Diana
Andersson, Helena
Mercado, Mónica Vázquez-Del
Chinoy, Hector
Lilleker, James B.
New, Paul
Krogh, Niels Steen
Lundberg, Ingrid
Alexanderson, Helene
MYONET Registry
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